Canonical Allele Identifier: CA373378543

Gene: NPR2

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.35805925C>T , CM000671.2:g.35805925C>T	GRCh38
NC_000009.11:g.35805922C>T , CM000671.1:g.35805922C>T	GRCh37
NC_000009.10:g.35795922C>T	NCBI36
NG_009249.1:g.18517C>T
NG_047141.1:g.11348G>A

Transcript Alleles

HGVS	Amino-acid Change
NM_003995.4:c.2143C>T MANE Select	NP_003986.2:p.Gln715Ter
ENST00000342694.7:c.2143C>T MANE Select	ENSP00000341083.2:p.Gln715Ter
NM_001378923.1:c.2152C>T	NP_001365852.1:p.Gln718Ter
NM_003995.3:c.2143C>T	NP_003986.2:p.Gln715Ter
ENST00000342694.6:c.2143C>T	ENSP00000341083.2:p.Gln715Ter
ENST00000421267.5:c.183C>T
ENST00000421267.6:c.183C>T
ENST00000448821.6:c.2143C>T	ENSP00000402902.2:p.Gln715Ter
ENST00000464810.5:n.2143C>T
ENST00000685871.1:c.2071C>T	ENSP00000509964.1:p.Gln691Ter
ENST00000686159.1:n.2182C>T
ENST00000686486.1:n.1313C>T
ENST00000687302.1:n.2257C>T
ENST00000687357.1:c.1996C>T	ENSP00000509549.1:p.Gln666Ter
ENST00000687625.1:n.1298C>T
ENST00000687787.1:c.2302C>T	ENSP00000509440.1:p.Gln768Ter
ENST00000688201.1:n.2100C>T
ENST00000688226.1:n.2075C>T
ENST00000688869.1:n.2449C>T
ENST00000689788.1:c.1937C>T	ENSP00000508973.1:n.1937C>T
ENST00000689898.1:c.2000C>T	ENSP00000509651.1:n.2000C>T
ENST00000690070.1:c.2227C>T	ENSP00000509654.1:p.Gln743Ter
ENST00000690267.1:c.1932C>T	ENSP00000510432.1:n.1932C>T
ENST00000690552.1:n.2004C>T
ENST00000691138.1:n.1932C>T
ENST00000691969.1:c.1643C>T	ENSP00000510244.1:n.1643C>T
ENST00000692232.1:n.3458C>T
ENST00000692233.1:c.2007C>T	ENSP00000509698.1:n.2007C>T
ENST00000692380.1:n.1298C>T
ENST00000692447.1:n.3259C>T
ENST00000693094.1:c.2143C>T	ENSP00000510161.1:p.Gln715Ter
XM_005251478.3:c.2152C>T	XP_005251535.1:p.Gln718Ter
XM_005251479.3:c.1165C>T	XP_005251536.1:p.Gln389Ter
XM_006716778.2:c.2080C>T	XP_006716841.1:p.Gln694Ter
XM_011517889.1:c.1165C>T	XP_011516191.1:p.Gln389Ter
XM_011517890.1:c.1165C>T	XP_011516192.1:p.Gln389Ter
XM_011517891.1:c.1165C>T	XP_011516193.1:p.Gln389Ter
XM_011517892.1:c.1165C>T	XP_011516194.1:p.Gln389Ter
XM_011517893.1:c.1165C>T	XP_011516195.1:p.Gln389Ter
XM_011517894.1:c.1165C>T	XP_011516196.1:p.Gln389Ter
XM_011517895.1:c.748C>T	XP_011516197.1:p.Gln250Ter
XM_024447556.1:c.2311C>T	XP_024303324.1:p.Gln771Ter
XM_024447557.1:c.2302C>T	XP_024303325.1:p.Gln768Ter
XM_024447558.1:c.1324C>T	XP_024303326.1:p.Gln442Ter
XM_024447559.1:c.907C>T	XP_024303327.1:p.Gln303Ter
XM_024447560.1:c.898C>T	XP_024303328.1:p.Gln300Ter
XM_024447561.1:c.739C>T	XP_024303329.1:p.Gln247Ter